|
| Status |
Public on Sep 12, 2013 |
| Title |
in vivo iPSC clone 445-1 |
| Sample type |
SRA |
| |
|
| Source name |
clone obtained from the blood of mouse ID#445
|
| Organism |
Mus musculus |
| Characteristics |
cell type: in vivo generated iPSC (passage 7) from a whole-body reprogrammable mouse transplanted with wt bone marrow
protocol: doxycycline-inducible OSKM lentivirus
transgenic line: reprogramming transgenic line B
|
| Growth protocol |
All iPSCs and ESCs were grown in DMEM supplemented with KSR 15% and LIF on feeder mouse fibroblasts.
|
| Extracted molecule |
total RNA |
| Extraction protocol |
Total RNA was extracted combining the Trizol reagent (Life Technologies) with the RNeasy Mini kit (Qiagen).
1 µg of total RNA samples was used as provided by the user. RNA Integrity Numbers were in the range 9.8 to 10 when assayed on an Agilent 2100 Bioanalyzer. PolyA+ fractions were purified and randomly fragmented, converted to double stranded cDNA and processed through subsequent enzymatic treatments of end-repair, dA-tailing, and ligation to adapters as in Illumina's "TruSeq Stranded mRNA Sample Preparation Part # 15031047 Rev. D" (this kit incorporates dUTP during 2nd strand cDNA synthesis, which implies that only the cDNA strand generated during 1st strand synthesis is eventually sequenced). Adapter-ligated library was completed by 9 cycles of PCR with Illumina PE primers. The resulting purified cDNA library of template molecules of known strand origin was applied to an Illumina flow cell for cluster generation (TruSeq cluster generation kit v5) and sequenced on the Genome Analyzer IIx with SBS TruSeq v5 reagents by following manufacturer's protocols.
|
| |
|
| Library strategy |
RNA-Seq |
| Library source |
transcriptomic |
| Library selection |
cDNA |
| Instrument model |
Illumina Genome Analyzer IIx |
| |
|
| Description |
Isolation of poly A+ RNA from total RNA
|
| Data processing |
Read files were quality-checked with FastQC.
Reads were aligned with the mouse genome (GRCm38/mm10) with TopHat-2.0.4 (using Bowtie 0.12.7 and Samtools 0.1.16), allowing 2 mismatches and 5 multihits.
Transcripts quantification and differential expression calculated with Cufflinks 1.3.0
Transcripts annotations used were Mus musculus GRCm38/mm10 from the UCSC Genome Browser
Genome_build: GRCm38/mm10
Supplementary_files_format_and_content: tables were generated with Cufflinks 1.3.0 and contain transcripts abundance measured in FPKM values
|
| |
|
| Submission date |
Jun 27, 2013 |
| Last update date |
May 15, 2019 |
| Contact name |
Manuel Serrano |
| E-mail(s) |
[email protected]
|
| Organization name |
IRB
|
| Department |
Molecular Medicine
|
| Lab |
Cellular Plasticity and Disease
|
| Street address |
Parc Científic de Barcelona, C/ Baldiri Reixac 10
|
| City |
Barcelona |
| State/province |
Barcelona |
| ZIP/Postal code |
08028 |
| Country |
Spain |
| |
|
| Platform ID |
GPL11002 |
| Series (1) |
| GSE48364 |
Transcriptional profiles by deep sequencing (RNA-seq) of in vivo-generated mouse iPSCs, in vitro-generated mouse iPSCs, and mouse ESCs |
|
| Relations |
| BioSample |
SAMN02214539 |
| SRA |
SRX316293 |
